Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → 3,5-Dichloro-4-(4-methoxyphenoxy)benzyl Alcohol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzenemethanol, 3,5-dichloro-4-hydroxy- | HCID 176409 | — |
| 반응물 | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| 촉매 | Cupric acetate | HCID 8895 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3,5-Dichloro-4-(4-methoxyphenoxy)benzyl Alcohol | HCID 22285654 | 44.8% |
반응 단계
To a flask containing 24 ml of dichloromethane was added 4 A sieves (2.97 g, activated at 500° C. for 8 h), 4-methoxyphenylboronic acid (1.84 g, 12.0 mmol), 2,6-dichloro-4-hydroxymethylphenol (465 mg, 2.41 mmol), copper (II) acetate (438 mg, 2.41 mmol), pyridine (0.97 ml, 12.0 mmol) and triethylamine (1.67 ml, 12.0 mmol). The reaction flask was fitted with a drying tube and stirred overnight. Filtration through celite and removal of volatiles in vacuo followed by column chromatography (silica, 30% ethyl acetate in hexane) provided the title compound as light brown oil (323 mg, 44%). 1H NMR (400 MHz, CDCl3) δ 7.39 (s, 2H), 6.82 (d, j=7.2 Hz, 2H), 6.77 (d, j=7.2 Hz, 2H), 4.69 (s, 2H), 3.76 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06967220B2 |
| 출처 데이터셋 | uspto-grants-2005_11 |
| ORD ID | ord-8bdd5a8db7ac4a48952c388ce2db5398 |
| 출처 메모 | uspto-grants-2005_11 |